A bile acid-like steroid modulates Caenorhabditis elegans lifespan through nuclear receptor signaling

被引:184
作者
Gerisch, Birgit
Rottiers, Veerle
Li, Dongling
Motola, Daniel L.
Cummins, Carolyn L.
Lehrach, Hans
Mangelsdorf, David J.
Antebi, Adam
机构
[1] Baylor Coll Med, Huffington Canc Aging, Dept Mol & Cellular Biol, Houston, TX 77030 USA
[2] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[3] Univ Texas, SW Med Ctr, Dept Pharmacol, Howard Hughes Med Inst, Dallas, TX 75390 USA
关键词
aging; DAF-12; hormone; dafachronic acid; germ-line longevity;
D O I
10.1073/pnas.0700847104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Broad aspects of Caenorhabditis elegans life history, including larval developmental timing, arrest at the dauer diapause, and longevity, are regulated by the nuclear receptor DAF-12. Endogenous DAF-12 ligands are 3-keto bile acid-like steroids, called dafachronic acids, which rescue larval defects of hormone-deficient mutants, such as daf-9/cytochrome P450 and daf-36/Rieske oxygenase, and activate DAF-12. Here we examined the effect of dafachronic acid on pathways controlling lifespan. Dafachronic acid supplementation shortened the lifespan of long-lived daf-9 mutants and abolished their stress resistance, indicating that the ligand is "proaging" in response to signals from the dauer pathways. However, the ligand extended the lifespan of germ-line ablated daf-9 and daf-36 mutants, showing that it is "antiaging" in the germ-line longevity pathway. Thus, dafachronic acid regulates C elegans lifespan according to signaling state. These studies provide key evidence that bile acid-like steroids modulate aging in animals.
引用
收藏
页码:5014 / 5019
页数:6
相关论文
共 29 条
[1]   Gene expression profile of long-lived Ames dwarf mice and Little mice [J].
Amador-Noguez, D ;
Yagi, K ;
Venable, S ;
Darlington, G .
AGING CELL, 2004, 3 (06) :423-441
[2]  
Antebi A, 2000, GENE DEV, V14, P1512
[3]  
Antebi A, 1998, DEVELOPMENT, V125, P1191
[4]   Cell nonautonomy of C-elegans daf-2 function in the regulation of diapause and life span [J].
Apfeld, J ;
Kenyon, C .
CELL, 1998, 95 (02) :199-210
[5]   Regulation of life-span by germ-line stem cells in Caenorhabditis elegans [J].
Arantes-Oliveira, N ;
Apfeld, J ;
Dillin, A ;
Kenyon, C .
SCIENCE, 2002, 295 (5554) :502-505
[6]   Germ-cell loss extends C-elegans life span through regulation of DAF-16 by kri-1 and lipophilic-hormone signaling [J].
Berman, JR ;
Kenyon, C .
CELL, 2006, 124 (05) :1055-1068
[7]  
Gems D, 1998, GENETICS, V150, P129
[8]   Hormonal signals produced by DAF-9/cytochrome P450 regulate C-elegans dauer diapause in response to environmental cues [J].
Gerisch, B ;
Antebi, A .
DEVELOPMENT, 2004, 131 (08) :1765-1776
[9]   A hormonal signaling pathway influencing C-elegans metabolism, reproductive development, and life span [J].
Gerisch, B ;
Weitzel, C ;
Kober-Eisermann, C ;
Rottiers, V ;
Antebi, A .
DEVELOPMENTAL CELL, 2001, 1 (06) :841-851
[10]   DAF-12-dependent rescue of dauer formation in Caenorhabditis elegans by (25S)-cholestenoic acid [J].
Held, Jason M. ;
White, Mark P. ;
Fisher, Alfred L. ;
Gibson, Bradford W. ;
Lithgow, Gordon J. ;
Gill, Matthew S. .
AGING CELL, 2006, 5 (04) :283-291